Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 4:89835580 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM981851

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4304, 2010_April_001_080_SNCA_163890_0002

HGVS names

This variant has 27 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and is associated with 2 phenotypes.

Variant displays